Variant (rsID / SNP)

rs72875762

rs72875762 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NDUFAF7, CEBPZ. Location: chromosome 2, position 37,458,898. Clinical significance in the table: Benign.

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Reference-table entries

NDUFAF7Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 2:37458898
Cytoband: 2p22.2
HGVS: NM_144736.5(NDUFAF7):c.50G>A (p.Arg17His)
Allele change: Missense_R17H

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.